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²éѯ½á¹û£º¹²²éµ½68¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . decursivine C20H16N2O4 ÏàËÆ¶È:59.0% Pharmaceutical Biology 2002 40 221-224 Antimalarial Agents from Plants II. Decursivine, A New Antimalarial Indole Alkaloid from Rhaphidophora decursiva Zhang H., Qiu S., Tamez P., Tan G.T., Aydogmus Z., Hung N.V., Cuong N.M., Angerhofer C., Doel Soejarto D., Pezzuto J.M., Fong H.H.S. Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . synthetic 8-oxyberberubine ÏàËÆ¶È:54.5% Molecules 2009 14 726-737 Total Syntheses of (¡À)-Gusanlung A, (¡À)-Gusanlung D and 8-Oxyberberrubine and the Uncertainty Concerning the Structures of (-)-Gusanlung A, (-)-Gusanlung D and 8-Oxyberberrubine Surachai Nimgirawath, Phansuang Udomputtimekakul, Thitima Apornpisarn, Asawin Wanbanjob and Thongchai Taechowisan Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (2,3-trans-3,4-cis)-3',4'-Methylenedioxy-3,4,5,6-tetramethoxy-[2'',3'':7,8]-furanoflavan ÏàËÆ¶È:54.5% Phytochemistry 1996 42 1459-1471 Twenty-three flavonoids from Lonchocarpus subglaucescens Aderbal F. Magalhães, Ana Maria G. Azevedo Tozzi, Beatriz Helena L. Noronha Sales, Eva G. Magalhães Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2-[(4,6,8-trimethylazulen-1-yl)diazenyl]-4-phenyl-1,3-thiazole C22H19N3S ÏàËÆ¶È:54.5% Journal of Heterocyclic Chemistry 2003 40 995-1004 Azulene-1-azo-2'-thiazoles. Synthesis and properties Alexandru C. Razus,Liviu Birzan,Stefania Nae,Mirela Nina Surugiu and Valentin Cimpeanu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 5,6-Methylenedioxy-1-(3,4-dimethoxybenzyl) isoquino-line C19H17O4 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 1996 4 781-791 Coralyne and related compounds as mammalian topoisomerase I and topoisomerase II poisons Darshan Makhey, Barbara Gatto, Chiang Yu, Angela Liu, Leroy F. Liu, Edmond J. LaVoie Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 6,7-Dimethoxy-1-methyl-3-(3,4-methylenedioxyphenyl)isoquinoline C19H17NO4 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 1996 4 781-791 Coralyne and related compounds as mammalian topoisomerase I and topoisomerase II poisons Darshan Makhey, Barbara Gatto, Chiang Yu, Angela Liu, Leroy F. Liu, Edmond J. LaVoie Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 3 C22H17NO7 ÏàËÆ¶È:54.5% Journal of Natural Products 2012 75 1578-1583 Cytotoxic Lignans from Fruits of Cleistanthus indochinensis: Synthesis of Cleistantoxin Derivatives Van Trinh Thi Thanh, Van Cuong Pham, Huong Doan Thi Mai, Marc Litaudon, Françoise Gu¨¦ritte, Pascal Retailleau, Van Hung Nguyen, and Van Minh Chau Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . butein-4-methoxyl-4'-O-(6''-O-acetyl)-¦Â-D-glucopyranoside C24H24O11 ÏàËÆ¶È:54.1% Chemical Research in Chinese Universities 2009 25 328-331 Constituents from Aerial Parts of Bidens ceruna L. and Their DPPH Radical Scavenging Activity ZHU Na, LI Xu-wen, LIU Gui-ying, SHI Xiao-lei, GUI Ming-yu,SUN Chang-qing and JIN Yong-ri Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (2S,3S)-5-O-¦Â-D-glucopyranosyloxy-6-methyl-4'-methoxy-3,7,4'-trihydroxyflavan C23H28O11 ÏàËÆ¶È:52.1% Journal of Natural Products 2002 65 262-266 New Phenolic Constituents from Smilax bracteata Shu Yuan Li, Hiroyuki Fuchino, Nobuo Kawahara, Setsuko Sekita, and Motoyoshi Satake Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . andropaniculoside A C23H24O11 ÏàËÆ¶È:52.1% Journal of Asian Natural Products Research 2008 10 17-24 Flavonoids and ent-labdane diterpenoids from Andrographis paniculata and their antiplatelet aggregatory and vasorelaxing effects TIAN-SHUNG WU, HUEI-JEN CHERN, AMOORU GANGAIAH DAMU,PING-CHUNG KUO, CHUNG-REN SU, E.-JIAN LEE and CHI-MING TENG Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 7,8-seco-holostylone B C21H22O7 ÏàËÆ¶È:50% Phytochemistry 2004 65 751-759 Aryltetralone lignans and 7,8-seco-lignans from Holostylis reniformis Tito da Silva, Lucia M.X. Lopes Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . rheediaxanthone A ÏàËÆ¶È:50% Phytochemistry 2003 467-470 Xanthones from the bark of Garcinia merguensis Lien-Hoa D. Nguyen, Hau T. Vo, Hung D. Pham, Joseph D. Connolly,Leslie J. Harrison Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 3 ÏàËÆ¶È:50% Phytochemistry 2002 59 851-856 Two highly oxygenated eudesmanes and 10 lignans from Achillea holosericea Ahmed A. Ahmed, Ahmed A. Mahmoud, Eptehal T. Ali, Olga Tzakou,Maria Couladis, Tom J. Mabry, Tam¨¢s G¨¢tid, G¨¢bor T¨®th Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 8-trichloromethyl-7,8-dihydropalmatine ÏàËÆ¶È:50% Journal of Natural Products 2003 66 481-486 Palmatine and Berberine Isolation Artifacts Radek Marek, Pavlna Sečkov, Dagmar Hulov, Jaromr Marek, Ji Dostl, and Vladimr Sklen Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 8-hydroxydihydroberberine ÏàËÆ¶È:50% Journal of Natural Products 2003 66 481-486 Palmatine and Berberine Isolation Artifacts Radek Marek, Pavlna Sečkov, Dagmar Hulov, Jaromr Marek, Ji Dostl, and Vladimr Sklen Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 2,3,9,10-dimethylenedioxy-8-oxoprotoberberine C19H13NO5 ÏàËÆ¶È:50% Planta Medica 2001 67 189-190 Isoquinoline Alkaloids from Thalictrum delavayi Mai Li, Xin Chen, Qin-Mei Tang, Jin-Sheng Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . machilusol B C20H22O6 ÏàËÆ¶È:50% Planta Medica 2000 66 403-407 Cytotoxic Neolignans from the Stem Wood of Machilus obovatifolia Ian-Lih Tsai,Jyh-Huey Chen,Chang-Yih Duh,Ih-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 5-hydroxytrachelogenin C21H24O8 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1980 28 850-860 Introduction of an Alcoholic Hydroxyl Group into 2, 3-Dibenzylbutyrolactone Lignans with Oxidizing Agents and Carbon-13 Nuclear Magnetic Resonance Spectra of the Oxidation Products SANSEI NISHIBE,MARIKO CHIBA,AKIYO SAKUSHIMA,SUEO HISADA,SAKAE YAMANOUCHI,MICHIO TAKIDO,USHIO SANKAWA and AKIRA SAKAKIBARA Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . licarin B ÏàËÆ¶È:50% Journal of Chinese Pharmaceutical Sciences 2005 14 137-139 A Benzofuranoid Neolignan from Magnolia biondii Pamp LU Yan-hua; GAO Yang; WANG Zheng-tao; LIU Jian-qun; and WEI Dong-zhi Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . demethoxyaschantin ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 1995 20 102-104 Biolgically Active Lignins from Magnolia bilndii Pamp Ma Yuliang and Han Guiqiu Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . leptopidinine C20H17NO6 ÏàËÆ¶È:50% Phytochemistry 1999 50 339-343 Five alkaloids from Hypecoum leptocarpum Yi Zhou, Guolin Zhang, Bogang Li Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . arizonicanol E ÏàËÆ¶È:50% Phytochemistry 1998 48 1187-1193 Isoflavonoids from Sophora secundiflora, S. arizonica and S. gypsophila Toshiyuki Tanaka, Masayosi Ohyama, Munekazu Iinuma, Yoshiaki Shirataki, Manki Komatsu, Charles L. Burandt Structure 13C NMR ̼Æ×Ä£Äâͼ |
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